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J Antimicrob Chemother ; 74(4): 1092-1100, 2019 04 01.
Artículo en Inglés | MEDLINE | ID: mdl-30561656

RESUMEN

OBJECTIVES: Rates of Clostridioides (Clostridium) difficile infection (CDI) are higher in North Wales than elsewhere in the UK. We used WGS to investigate if this is due to increased healthcare-associated transmission from other cases. METHODS: Healthcare and community C. difficile isolates from patients across North Wales (February-July 2015) from glutamate dehydrogenase (GDH)-positive faecal samples underwent WGS. Data from patient records, hospital management systems and national antimicrobial use surveillance were used. RESULTS: Of the 499 GDH-positive samples, 338 (68%) were sequenced and 299 distinct infections/colonizations were identified, 229/299 (77%) with toxin genes. Only 39/229 (17%) toxigenic isolates were related within ≤2 SNPs to ≥1 infections/colonizations from a previously sampled patient, i.e. demonstrated evidence of possible transmission. Independent predictors of possible transmission included healthcare exposure in the last 12 weeks (P = 0.002, with rates varying by hospital), infection with MLST types ST-1 (ribotype 027) and ST-11 (predominantly ribotype 078) compared with all other toxigenic STs (P < 0.001), and cephalosporin exposure in the potential transmission recipient (P = 0.02). Adjusting for all these factors, there was no additional effect of ward workload (P = 0.54) or failure to meet cleaning targets (P = 0.25). Use of antimicrobials is higher in North Wales compared with England and the rest of Wales. CONCLUSIONS: Levels of transmission detected by WGS were comparable to previously described rates in endemic settings; other explanations, such as variations in antimicrobial use, are required to explain the high levels of CDI. Cephalosporins are a risk factor for infection with C. difficile from another infected or colonized case.


Asunto(s)
Clostridioides difficile/genética , Infecciones por Clostridium/epidemiología , Infecciones por Clostridium/transmisión , Secuenciación Completa del Genoma , Clostridioides difficile/efectos de los fármacos , Infecciones por Clostridium/historia , Infecciones por Clostridium/microbiología , Heces/química , Heces/microbiología , Femenino , Geografía Médica , Historia del Siglo XXI , Humanos , Incidencia , Masculino , Epidemiología Molecular , Vigilancia en Salud Pública , Factores de Riesgo , Gales/epidemiología
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